Disease: Waist Circumference
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 16
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 14
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 12
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 11
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 10
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 9
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 9
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 9
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 8
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 8
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 8
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 8
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 7
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 7
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 7
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 7